Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1711863893
Device Listing 1711863893
Listing Summary
#
Listing key
1711863893
Premarket submission
DEN170072
Device
Enlight 1810
Applicant
Timpel, Inc.
Product code
QEB
Decision date
2018-12-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
237237
3016509761
3016509761
TIMPEL S.A.
1
N
2026-01-01
Rua Jose Leonardi 280 Bloco A Pato Branco Parana BR 85503